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The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy.
Pierpont, Elizabeth I; Bennett, Anton M; Schoyer, Lisa; Stronach, Beth; Anschutz, April; Borrie, Sarah C; Briggs, Benjamin; Burkitt-Wright, Emma; Castel, Pau; Cirstea, Ion C; Draaisma, Fieke; Ellis, Michelle; Fear, Vanessa S; Frone, Megan N; Flex, Elisabetta; Gelb, Bruce D; Green, Tamar; Gripp, Karen W; Khoshkhoo, Sattar; Kieran, Mark W; Kleemann, Karolin; Klein-Tasman, Bonita P; Kontaridis, Maria I; Kruszka, Paul; Leoni, Chiara; Liu, Clifford Z; Merchant, Nadia; Magoulas, Pilar L; Moertel, Christopher; Prada, Carlos E; Rauen, Katherine A; Roelofs, Renée; Rossignol, Rodrigue; Sevilla, Christine; Sevilla, Gigi; Sheedy, Ryan; Stieglitz, Elliot; Sun, Daochun; Tiemens, Dagmar; White, Forest; Wingbermühle, Ellen; Wolf, Cordula; Zenker, Martin; Andelfinger, Gregor.
  • Pierpont EI; Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
  • Bennett AM; Department of Pharmacology, Yale School of Medicine, New Haven, Connecticut, USA.
  • Schoyer L; RASopathies Network, Los Angeles, California, USA.
  • Stronach B; RASopathies Network, Los Angeles, California, USA.
  • Anschutz A; RASopathies Network, Los Angeles, California, USA.
  • Borrie SC; KU Leuven, Laboratory for the Research of Neurodegenerative Diseases, Leuven, Belgium.
  • Briggs B; School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
  • Burkitt-Wright E; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust and University of Manchester, Manchester, UK.
  • Castel P; Department of Biochemistry & Molecular Pharmacology, NYU Grossman School of Medicine, New York, New York, USA.
  • Cirstea IC; Institute of Comparative Molecular Endocrinology, Ulm University, Ulm, Germany.
  • Draaisma F; Institute of Applied Physiology, Ulm University, Ulm, Germany.
  • Ellis M; Department of Pediatrics, Radboud Institute for Health Sciences, Radboud University Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands.
  • Fear VS; RASopathies Network, Los Angeles, California, USA.
  • Frone MN; Translational Genetics, Precision Health, Telethon Kids Institute, The University of Western Australia, Perth, Western Australia, Australia.
  • Flex E; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Bethesda, Maryland, USA.
  • Gelb BD; Department of Oncology and Molecular Medicine, Instituo Superiore di Sanità, Rome, Italy.
  • Green T; Mindich Child Health and Development Institute and the Departments of Pediatrics and Genetics and Genomic Sciences, Icahn School of Medicine, New York, New York, USA.
  • Gripp KW; Division of Interdisciplinary Brain Sciences, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, USA.
  • Khoshkhoo S; Division of Medical Genetics, Department of Pediatrics, Nemours Children's Hospital, Orlando, Florida, USA.
  • Kieran MW; Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Kleemann K; Research and Development, Day One Biopharmaceuticals, Brisbane, California, USA.
  • Klein-Tasman BP; Clinic for Cardiothoracic and Vascular Surgery, University Medical Center Göttingen, Göttingen, Germany.
  • Kontaridis MI; German Center for Cardiovascular Research (DZHK), Partner Site Göttingen, Göttingen, Germany.
  • Kruszka P; Department of Psychology, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin, USA.
  • Leoni C; Department of Biomedical Research and Translational Medicine, Masonic Medical Research Institute, Utica, New York, USA.
  • Liu CZ; Division of Cardiology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Merchant N; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts, USA.
  • Magoulas PL; GeneDx, Gaithersburg, Maryland, USA.
  • Moertel C; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A.Gemelli, IRCCS, Rome, Italy.
  • Prada CE; Mindich Child Health and Development Institute and the Departments of Pediatrics and Genetics and Genomic Sciences, Icahn School of Medicine, New York, New York, USA.
  • Rauen KA; Division of Endocrinology, Children's National Hospital, Washington, DC, USA.
  • Roelofs R; Department of Molecular and Human Genetics, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
  • Rossignol R; Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
  • Sevilla C; Division of Genetics, Genomics, and Metabolism, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
  • Sevilla G; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Sheedy R; Department of Pediatrics, Division of Genomic Medicine, University of California, Davis, Davis, California, USA.
  • Stieglitz E; Centre of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands.
  • Sun D; Rare Diseases, Genetics and Metabolism, University of Bordeaux, Bordeaux, France.
  • Tiemens D; Parent Advocate, CFC Syndrome, Lombard, Illinois, USA.
  • White F; Self Advocate, CFC Syndrome, Lombard, Illinois, USA.
  • Wingbermühle E; Parent Advocate, Costello Syndrome, Centerton, Arkansas, USA.
  • Wolf C; Department of Pediatrics, Benioff Children's Hospital, University of California, Oakland, California, USA.
  • Zenker M; Cancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Andelfinger G; Department of Pediatrics, Radboud Institute for Health Sciences, Radboud University Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands.
Am J Med Genet A ; 194(4): e63477, 2024 Apr.
Article en En | MEDLINE | ID: mdl-37969032
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Displasia Ectodérmica / Síndrome de Costello / Cardiopatías Congénitas / Neoplasias / Síndrome de Noonan Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Displasia Ectodérmica / Síndrome de Costello / Cardiopatías Congénitas / Neoplasias / Síndrome de Noonan Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article